Yen Elizabeth, Kaneko-Tarui Tomoko, Maron Jill L
Mother Infant Research Institute at Tufts Medical Center, Boston, MA, United States.
Division of Newborn Medicine, Tufts Children's Hospital, Boston, MA, United States.
Front Pediatr. 2021 Jan 26;8:618553. doi: 10.3389/fped.2020.618553. eCollection 2020.
Non-invasive techniques to monitor and diagnose neonates, particularly those born prematurely, are a long-sought out goal of Newborn Medicine. In recent years, technical advances, combined with increased assay sensitivity, have permitted the high-throughput analysis of multiple biomarkers simultaneously from a single sample source. Multiplexed transcriptomic and proteomic platforms, along with more comprehensive assays such as RNASeq, allow for interrogation of ongoing physiology and pathology in unprecedented ways. In the fragile neonatal population, saliva is an ideal biofluid to assess clinical status serially and offers many advantages over more invasively obtained blood samples. Importantly, saliva samples are amenable to analysis on emerging proteomic and transcriptomic platforms, even at quantitatively limited volumes. However, biomarker targets are often degraded in human saliva, and as a mixed source biofluid containing both human and microbial targets, saliva presents unique challenges for the investigator. Here, we provide insight into technical considerations and protocol optimizations developed in our laboratory to quantify and discover neonatal salivary biomarkers with improved reproducibility and reliability. We will detail insights learned from years of experimentation on neonatal saliva within our laboratory ranging from salivary collection techniques to processing to downstream analyses, highlighting the need for consistency in approach and a global understanding of both the potential benefits and limitations of neonatal salivary biomarker analyses. Importantly, we will highlight the need for robust and stringent research in this population to provide the field with standardized approaches and workflows to impact neonatal care successfully.
监测和诊断新生儿,尤其是早产儿的非侵入性技术,是新生儿医学长期以来追求的目标。近年来,技术进步与检测灵敏度的提高相结合,使得能够从单一样本来源同时对多种生物标志物进行高通量分析。多重转录组学和蛋白质组学平台,以及诸如RNA测序等更全面的检测方法,使我们能够以前所未有的方式探究正在发生的生理和病理情况。在脆弱的新生儿群体中,唾液是一种理想的生物流体,可用于连续评估临床状态,与通过更具侵入性获得的血液样本相比具有许多优势。重要的是,即使唾液样本的数量有限,也适合在新兴的蛋白质组学和转录组学平台上进行分析。然而,生物标志物靶点在人类唾液中往往会降解,而且作为一种包含人类和微生物靶点的混合来源生物流体,唾液给研究人员带来了独特的挑战。在此,我们深入探讨了我们实验室为量化和发现具有更高重现性和可靠性的新生儿唾液生物标志物而制定的技术考量和方案优化。我们将详细介绍从我们实验室多年来对新生儿唾液的实验中获得的见解,从唾液采集技术到处理再到下游分析,强调方法一致性的必要性以及对新生儿唾液生物标志物分析的潜在益处和局限性的全面理解。重要的是,我们将强调在这一人群中进行稳健和严格研究的必要性,以便为该领域提供标准化的方法和工作流程,从而成功影响新生儿护理。